19 Replies
@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.ans B hai ??
proper explanation mile toh ping
yeah
cl leaving grp
carbocation formation
n has lone pair and it is less strained than o in ring so ig vaha add hoga
cl ko leave karayega kaun
hnn vo baat hai
hai?? wont it be sn2
with N cuz N better lone pair donator right
uhh lemme think ik min
Yep I think the acid base logic applies here.
But I am oc noob. Will wait for others to chime in :)
You see two nucleophilic sites?
N and O
Which is more nucleophilic?
N
‘cause less electronegativity
You see an electrophile
What’s that?
Acid chloride
Attack it with the better nucleophile
What do you get?
B)
sanchep me humne yahi bola
bas mera sn1 ya sn2 glt ho sakta hai
yar ye esterification nahi ha
ye hume likhvai thi
yaha ester thodi ban rha
Yaar tum khud batayo
Jyada nucleophilic kya hai?
N ya O?
N
ye rxn yaad krne ka koi fayda nahi mene dekhlia
Bas fir electrophile pe vo attack karega
Bas kuch reactions hain jinka mechanism nahi hai syll me
Vo yaad rakho
okayy
+solved @Enamine
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